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CS-W001157 4
Total: USD 88.00

3-Bromo-4-iodopyridine

  • CAS No. 89167-19-1

  • Cat. No. CS-0041168
  • Purity≥95%
  • MDL No.MFCD11110263

*For research and further manufacturing use only, not for direct human use.

3-Bromo-4-iodopyridine|CS-0041168

Structure of 89167-19-1

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General Information

  • CAS No. 89167-19-1
  • Cat. No. CS-0041168
  • Purity ≥95%
  • MDL No. MFCD11110263
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₃BrIN
  • Molecular Weight 283.89
  • Synonym(s) pyridine, 3-bromo-4-iodo-
  • SMILES IC1=C(Br)C=NC=C1

Description

3-Bromo-4-iodopyridine is a heteroaromatic dihalogenated pyridine featuring complementary halogen handles for cross-coupling reactions. The bromine and iodine substituents enable sequential functionalization via palladium-catalyzed processes, offering strategic control in synthetic sequence design. This electron-deficient scaffold integrates efficiently into complex molecular architectures under standard conditions.

Application

3-Bromo-4-iodopyridine serves as a versatile building block in cross-coupling chemistry, enabling efficient construction of substituted pyridine scaffolds. The complementary halogenation pattern facilitates sequential Pd-catalyzed coupling reactions, with bromide typically reacting first under standard conditions. Its bench-stable nature and predictable reactivity support reliable functionalization in medicinal chemistry and materials synthesis workflows.

Synthesis

  • Route1

    References

    • Baxter, Paul N. W. Chemistry - A European Journal, 2003 , vol. 9, # 11 p. 2531 - 2541
  • Route2

    References

    • Chemistry - A European Journal, , vol. 17, # 47 p. 13284 - 13297

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   12.89
  • LogP   2.4487
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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